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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036212Generated: November 2, 2026

Trifluoroacetic acid → HCID 58447649, compound

https://huagongshe.com/reaction/1036212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 2-(3-methyl-4-(pyridazin-4-yl)phenyl)acetateHCID 58447683—
SolventDichloromethaneHCID 6344—
ProductHCID 58447649HCID 58447649—

Reaction Steps

The ester 134-2 obtained in step 2 was stirred in DCM (15 ml) with trifluoroacetic acid (TFA, 3 ml) at room temperature overnight. After concentrated by evaporation, the residue was redistributed between ethyl acetate (30 ml) and 5% Na2CO3 aqueous solution (30 ml). The aqueous phase was acidified to pH around 2 with 6 N HCl solution and extracted with ethyl acetate (40 ml×2). The organic extraction was evaporated to give 2-(3-methyl-4-(pyridazin-4-yl)phenyl)acetic acid 134-3 as a solid which is used for reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546396B2
Source datasetuspto-grants-2013_10
ORD IDord-dae847b2d20d4af3b2cae0d545dd6e28
Source noteuspto-grants-2013_10